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Article

[Study of oculomotor disorders in spinocerebellar ataxia genotype].

Nihon Jibiinkoka Gakkai kaiho - 1 Jan 2006

Oda Rie, Takemoto Tsuyoshi, Kawai Motoharu, Yamashita Hiroshi

Abstract excerpt

Spinocerebellar degeneration (SCD) exhibits a variety of spinal and cerebullar symptoms and progress. The recent advent of molecular genetics has revealed triplet repeat mutation in the gene of SCD patients. Due to the underlying genetic defects, hereditary SCD is referred to as different spinocerebellar ataxia (SCA) genotypes. We conducted vestibular functional tests in 33 SCD patients, including 3 with SCA3 and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16480004
DOI: 10.3950/jibiinkoka.109.30

Genes

SCD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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